Trials / Completed
CompletedNCT02455661
Femoral Closure Versus Radial Compression Devices Related to Percutaneous Coronary Interventions Study
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 600 (actual)
- Sponsor
- Universitätsmedizin Mannheim · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
FERARI is a single centre observational study comparing patients undergoing PCI either using radial compression devices or femoral closure devices at the corresponding access site. First primary outcomes consist of the occurrence of vascular complications at the arterial access site including major bleedings as defined by common classification systems Second primary outcomes consist of the occurrence of adverse cardiac events including all-cause mortality, target lesion and vessel revascularization (TLR and TVR) during 30 days and 12 months of follow-up.
Conditions
- Arterial Closure Device
- Percutaneous Coronary Intervention (PCI)
- Access Site Bleeding
- Adverse Cardiac Events
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | TR Band (TM) | |
| DEVICE | AngioSeal | |
| DEVICE | StarClose |
Timeline
- Start date
- 2014-02-01
- Primary completion
- 2018-05-01
- Completion
- 2019-10-01
- First posted
- 2015-05-28
- Last updated
- 2019-11-01
Locations
1 site across 1 country: Germany
Source: ClinicalTrials.gov record NCT02455661. Inclusion in this directory is not an endorsement.